A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4198



Internal ID15202197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:2091126..2117779hg38UCSC Ensembl
Outerchr4:2092853..2119506hg19UCSC Ensembl
Outerchr4:2062651..2089304hg18UCSC Ensembl
Outerchr4:2060084..2086737hg17UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3811984
hg1911984
hg1811984
hg1711984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7062
SamplesNA12156
Known GenesPOLN
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv4198
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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